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reduce animal usage in preclinical research

 

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Preclinical animal research is a necessity for the development of life-saving medicines. Microsampling technology offers several advantages for PK/PD, toxicity and efficacy studies, such as decreased costs and improved data quality.

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Hoping to humanize your animal studies? Achieving the 3Rs of animal research just got easier! This VAMS™ resource compilation includes case studies that provide details about the ability of microsampling technology to deliver:  

  • Sevenfold reduction in animal usage in research studies 
  • A pharmacokinetic (PK) profile from a single animal
  • Consistent, robust collection of 10 µL blood samples
  • Data that bridges to the plasma gold standard
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Compared to wet blood collection from rodents and other laboratory animals, dried blood microsampling is simpler, more ethical, more economical, and more effective.

  • Significantly reduce animal usage and comply with the 3Rs
  • Generate cleaner data due to reduced animal stress
  • Improve data consistency by reducing inter-animal variability
  • Eliminate dependence on satellite populations
  • Eliminate steps, processing, and equipment without sacrificing data quality

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Save Time, Save Labor, Promote The 3Rs

Easy to Use

A less stressful animal experience helps preserve the integrity of the data, and abiding by animal research ethics is less stressful for staff, too.

Simplify

Microsampling eliminates the need for mouse blood collection tubes, clips, and other equipment. Simplify collection and your entire workflow.

Reduce / Refine / Replace

Mitra microsampling promotes the ethical reduction of animals used in research and refines blood collection from animals.

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Mitra® is an exempt medical device in the US, CE-IVD self-certified in the UK and EU, a Class 1 IVD in Australia, and registered with Health Canada. It is intended as a specimen collector and for the storage and transport of biological fluids. Use of the device with blood for diagnostic applications is limited to certain countries and, in the US, for research and non-diagnostic purposes only. Neoteryx Products are not marketed in the US for clinical diagnostic uses. In other countries, Neoteryx Products may be used in clinical diagnostic laboratory systems after the laboratory has validated their complete system in compliance with relevant rules and regulations. Neoteryx operates a Quality Management System (QMS) that is based on FDA good manufacturing practices, 21 CFR 820 regulations, and ISO-13485.

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